Canonical Allele Identifier: CA136219472

Gene: SLC17A1

Linked Data

• dbSNP Id: rs1003988826
• MyVariant Identifiers: chr6:g.25787812T>C (hg19) ; chr6:g.25787584T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.25787584T>C , CM000668.2:g.25787584T>C	GRCh38
NC_000006.11:g.25787812T>C , CM000668.1:g.25787812T>C	GRCh37
NC_000006.10:g.25895791T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244527.10:c.*3-4366A>G MANE Select	ENSP00000244527.4:n.*3-4366A>G
ENST00000244527.8:c.*3-4366A>G	ENSP00000244527.4:n.*3-4366A>G
ENST00000377886.6:c.*658-4366A>G	ENSP00000367118.2:n.*658-4366A>G
NM_005074.3:c.*3-4366A>G	NP_005065.2:n.*3-4366A>G
XM_011514818.1:c.1179-4366A>G	XP_011513120.1:n.1179-4366A>G
XM_011514818.2:c.1329-4366A>G	XP_011513120.2:n.1329-4366A>G
XM_017011200.1:c.*3-4366A>G	XP_016866689.1:n.*3-4366A>G
XM_017011201.2:c.*2+11199A>G	XP_016866690.1:n.*2+11199A>G
NM_005074.5:c.*3-4366A>G MANE Select	NP_005065.2:n.*3-4366A>G